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Autor:
Bert B.A. de Vries, Lodewijk A. Sandkuijl, Kirsten Gelsema, Hugo J. Duivenvoorden, Monique van Rijn, Dicky J.J. Halley, S. Mohkamsing, Ben A. Oostra, Ans M.W. van den Ouweland, Martinus F. Niermeijer, Aad Tibben, Esther Mol
Publikováno v:
The American Journal of Human Genetics. (3):660-667
SummaryThe fragile X syndrome is an X-linked mental retardation disorder caused by an expanded CGG repeat in the first exon of the fragile X mental retardation (FMR1) gene. Its frequency, X-linked inheritance, and consequences for relatives all promp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbe1b487c89558683962791c187a0e46
